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Diclofenac sodium salt, Thermo Scientific Chemicals
Standard NSAID and cyclooxygenase (COX) inhibitor
$69.41 - $467.42
Chemical Identifiers
CAS | 15307-79-6 |
---|---|
Molecular Formula | C14H10Cl2NNaO2 |
Molecular Weight (g/mol) | 318.129 |
MDL Number | MFCD00082251 |
InChI Key | KPHWPUGNDIVLNH-UHFFFAOYSA-M |
Synonym | diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon |
PubChem CID | 5018304 |
ChEBI | CHEBI:4509 |
IUPAC Name | sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate |
SMILES | C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+] |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAJ6260906
|
Thermo Scientific Chemicals
J6260906 |
5 g |
Each for $69.41
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AAJ6260914
|
Thermo Scientific Chemicals
J6260914 |
25 g |
Each for $153.49
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AAJ6260922
|
Thermo Scientific Chemicals
J6260922 |
100 g |
Each for $467.42
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Description
Oxidation of diclofenac sodium produces the metabolite 4'-hydroxy diclofenac) which demonstrates specific inhibition of Cox-2. Inhibition of Cox by diclofenac and 4'-hydroxy diclofenac suppresses prostaglandin E2 synthesis, producing anti-inflammatory and analgesic effects. Diclofenac is also shown to stabilize the native tetrameric conformation of transthyretin (TTR) fibrils, preventing the formation of insoluble amyloidogenic TTR deposits. Diclofenac Sodium is a substrate of CYP2C9. It is also used as an inhibitor of Cox-1 and Cox-2.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsOxidation of diclofenac sodium produces the metabolite 4′-hydroxy diclofenac) which demonstrates specific inhibition of Cox-2. Inhibition of Cox by diclofenac and 4′-hydroxy diclofenac suppresses prostaglandin E2 synthesis, producing anti-inflammatory and analgesic effects. Diclofenac is also shown to stabilize the native tetrameric conformation of transthyretin (TTR) fibrils, preventing the formation of insoluble amyloidogenic TTR deposits. Diclofenac Sodium is a substrate of CYP2C9. It is also used as an inhibitor of Cox-1 and Cox-2.
Solubility
Soluble in water (50 mg/ml), PBS pH 7.2 (6 mg/ml), ethanol (∼35 mg/ml), DMF (∼35 mg/ml), DMSO (∼35 mg/ml), methanol (>24 mg/ml), and acetone (6 mg/ml).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
Chemical Identifiers
15307-79-6 | |
318.129 | |
KPHWPUGNDIVLNH-UHFFFAOYSA-M | |
5018304 | |
sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate |
C14H10Cl2NNaO2 | |
MFCD00082251 | |
diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon | |
CHEBI:4509 | |
C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+] |
Specifications
15307-79-6 | |
White | |
MFCD00082251 | |
UN2811 | |
diclofenac sodium, sodium diclofenac, diclofenac sodium salt, voltaren, solaraze, anthraxiton, prophenatin, allvoran, batafil, delimon | |
KPHWPUGNDIVLNH-UHFFFAOYSA-M | |
sodium;2-[2-(2,6-dichloroanilino)phenyl]acetate | |
5018304 | |
318.14 | |
Diclofenac sodium salt |
283°C to 285°C | |
C14H10Cl2NNaO2 | |
5 g | |
14,3081 | |
Soluble in water to 50mg/ml. | |
C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[Na+] | |
318.129 | |
CHEBI:4509 | |
Powder |
Safety and Handling
GHS H Statement
H301-H361
Toxic if swallowed.
Suspected of damaging fertility or the unborn child.
P264b-P270-P301+P310-P330-P501c
H301
DOTInformation : Transport Hazard Class: 6.1; Packing Group: III; Proper Shipping Name: TOXIC SOLIDS, ORGANIC, N.O.S.
EINECSNumber : 239-346-4
RTECSNumber : AG6330000
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only